Substituted ureidophenyl thioureas

ABSTRACT

UREIDOPHENYL THIOUREAS OF THE FORMULA:   1-(R-OOC-NH-C(=S)-NH-),2-(R&#34;-N(-R&#39;&#39;&#34;)-CO-N(-R&#39;&#39;)-),(X)N-   BENZENE   IN WHICH   EACH X INDEPENDENTLY STANDS FOR A HALOGEN ATOM, ALKYL WITH 1-4 CARBON ATOMS OR ALKOXY WITH 1-4 CARBON ATOMS, N STANDS FOR 0, 1 OR 2, R STANDS FOR ALKYL WITH 1-12 CARBON ATOMS, R&#39;&#39; AND R&#34; EACH STANDS INDEPENDENTLY FOR A HYDROGEN ATOM OR ALKYL WITH 1-4 CARBON ATOMS, AND R&#34;&#39;&#39; STANDS FOR A HYDROGEN ATOM, ALKYL WITH 1 OR 2 CARBON ATOMS (WHICH MAY CARRY AT LEAST ONE SUBSTITUENT SELECTED FROM HALOGEN, CYANO, ALKOXY WITH UP TO 4 CARBON ATOMS AND ALKOXYCARBONYL WITH UP TO 5 CARBON ATOMS), ALKYL WITH 3 TO 18 CARBON ATOMS (WHICH CARRIES AT LEAST ONE SUBSTITUENT SELECTED FROM HALOGEN, CYANO, ALKOXY WITH UP TO 4 CARBON ATOMS AND ALKOXYCARBONYL WITH UP TO 5 CARBON ATOMS), CYCLOALKYL WITH 5 TO 8 RING CARBON ATOMS, ARALKYL (THE ARYL MOIETY OF WHICH MAY CARRY AT LEAST ONE SUBSTITUENT SELECTED FROM HALOGEN, LOWER ALKYL AND LOWER ALKOXY), PHENYL (WHICH MAY CARRY AT LEAST ONE SUBSTITUENT SELECTED FROM HALOGEN, LOWER ALKYL AND LOWER ALKOXY), ACYL WITH UP T O 18 CARBON ATOMS (WHICH MAY BE SUBSTITUTED BY HALOGEN AND/OR LOWER ALKYL, AROYL (WHICH MAY CARRY AT LEAST ONE SUBSTITUENT SELECTED FROM HALOGEN, LOWER ALKYL AND LOWER A LKOXY), ALKYLSULFONYL WITH UP TO 18 CARBON ATOMS, ARYLSULFONYL (WHICH MAY CARRY AT LEAST ONE SUBSTITUENT SELECTED FROM HALOGEN, AMINO, LOWER ALKYL AND LOWER ALKOXY) OR IDALKYLAMINO WITH UP TO 4 CARBON ATOMS, WHICH POSSESS FUNGICIDAL PROPERTIES AND WHICH MAY BE PRODUCED BY CONVENTIONAL METHODS.

United States Patent 3,780,089 SUBSTITUTED UREIDOPHENYL THIOUREAS Arno Widdig, Blecher, Engelbert Kuhle, Bergisch Gladbach, Klaus Sasse, Schildgen, Hans Scheinpflug, Leverkusen, Ferdinand Grewe, Burscheid, and Helmut Kaspers and Paul-Ernst Frohberger, Leverknsen, Germany, assignors to Bayer Aktiengeselschaft, Leverkusen, Germany No Drawing. Filed Nov. 13, 1970, Ser. No. 89,500 Claims priority, application Germany, Nov. 29, 1969,

P 19 60 029.4 Int. Cl. C07c 157/06 US. Cl. 260-470 4 Claims ABSTRACT OF THE DISCLOSURE Ureidophenyl thioureas of the formula:

in which each X independently stands for a halogen atom, alkyl with 1-4 carbon atoms or alkoxy with 1-4 carbon atoms,

n stands for 0, l or 2,

R stands for alkyl with 1-12 carbon atoms,

R and R" each stands independently for a hydrogen atom or alkyl with 1-4 carbon atoms, and

R stands for a hydrogen atom, alkyl with 1 or 2 carbon atoms (which may carry at least one substituent selected from halogen, cyano, alkoxy with up to 4 carbon atoms and alkoxycarbonyl with up to carbon atoms), alkyl with 3 to 18 carbon atoms (which carries at least one substituent selected from halogen, cyano, alkoxy with up to 4 carbon atoms andalkoxycarbonyl with up to 5 carbon atoms), cycloalkyl with 5 to 8 ring carbon atoms, aralkyl (the aryl moiety of which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), phenyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), acyl with up to 18 carbon atoms (which may be substituted by halogen and/or lower alkyl), aroyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), alkylsulfonyl with up to 18 carbon atoms, arylsulfonyl (which may carry at least one substituent selected from halogen, amino, lower alkyl and lower alkoxy) or dialkylamino with up to 4 carbon atoms, which possess fungicidal properties and which may be produced by conventional methods.

The present invention relates to and has for its objects the provision of particular new ureidophenyl thioureas, which possess fungicidal properties, active compositions 3,780,089 Patented Dec. 18, 1973 in the form of mixtures of such compounds with solid and liquid dispersible carrier vehicles, and methods for producing such compounds and for using such compounds in a new way especially for combating fungi, with other and further objects becoming apparent from a study of the within specification and accompanying examples.

The present invention provides ureidophenylthioureas of the general formula in which each X independently stands for a halogen atom, alkyl with 1-4 carbon atoms or alkoxy with 1-4 carbon atoms,

n stands for 0, 1 or 2,

R stands for alkyl with 1-12 carbon atoms,

R and R" each stands independently for a hydrogen atom or alkyl with 1-4 carbon atoms and,

R'" stands for a hydrogen atom, alkyl with 1 or 2 carbon atoms (which may carry at least one substituent selected from halogen, cyano, a lkoxy with up to 4 carbon atoms and alkoxycarbonyl with up to 5 carbon atoms), alkyl with 3 to 18 carbon atoms (which carries at least one substituent selected from halogen, cyano, alltoxy with up to 4 carbon atoms and alkoxycarbonyl with up to 5 carbon atoms), cycloalkyl with 5 to 8 ring carbon atoms, aralkyl (the aryl moiety of which may carry at least one substituent selected from halogen,

lower alkyl and lower alkoxy), phenyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), acyl with up to 18 carbon atoms (which may be substituted by halogen and/ or lower alkyl), aroyl (which may carry at least one substituent selected from halogen, lower alkyl and lower alkoxy), al'kylsulfonyl with up to 18 carbon atoms, arylsulfonyl (which may carry at least one substituent selected from halogen, amino, lower alkyl and lower aikoxy) or dialkylamino with up to 4 carbon atoms.

The compounds of the Formula I have beenv found to exhibit strong fungicidal properties.

The invention also provides a process for the production of the ureidophenylthioureas of the Formula I in which a 2-ureidoaniline derivative of the formula NH: R1"

-'N-o 0-n 3 inwhich X, n, R, R", and R' have the meanings stated above,

is reacted with an isothiocyanate of the formula in which R has the meaning stated above,

in the presence of a diluent (which term herein includes a solvent).

It is surprising that the ureidophenylthioureas of the Formula I exhibit a higher fungicidal activity than zinc ethylene 1,2 bis-dithiocarbamate. The active compound according to the invention therefore represent an enrichment of the art.

When N-2-aminophenyl-N'-methylurea and ethoxy carbonylisothiocyanate are used as starting materials, the reaction course can be represented by the following equation:

8 nn-li-nn-ooocnr,

The 2-ureidoaniline derivatives used as starting materials are defined by the Formula II. In this formula, as in Formula I, X stands preferably for chlorine, bromine, fluorine, methyl, ethyl, isopropyl, n-butyl, methoxy, ethoxy or isoproxy; n stands preferably for the numbers or 1; R and R" stand preferably for hydrogen, methyl or ethyl, R" stands preferably for hydrogen, alkyl with 1 or 2 carbon atoms, substituted alkyl with 1 to 12 carbon atoms, benzyl, phenyl, p-tolyl, p-methoxyphenyl, methoxyethyl, ethoxypropyl, cyanopentyl, acetyl, benzoyl, methanesulfonyl, p-toluenesulfonyl or dimethylamino.

As examples of the 2-ureidoaniline derivatives, there may be mentioned: 2-amino-phenylurea, N-2-aminophenyl-N'-methylurea, N-2-aminophenyl-N', -dimethylurea, N-2-aminophenyl-N-O-cyanopentyl-urea, N 2 aminophenyl-N'2-methoxy ethylurea, N-2 aminophenyl-N'- benzylurea, N-2-aminophenyl-N'-phenylurea, N-2-aminophenyl-N-acetylurea, N-2 aminophenyl-N'-benzoylurea, N-Z-aminophenyl-N'-p-toluenesulfonylurea, 4 (Z-aminophenyl)-1,I-dimethylsemicarbazide, and the like.

The Z-ureido-anilines used as starting materials are partially known (see Beilsteins Handbuch der organischen Chemie, Volume 13, pages 20-32, Berlin, 1930; Volume 13 (1) Erganzungswerk (1st Supplement), pages 8-10, Berlin, 1933; Volume 13 (2) Erganzungswerk (2nd Supplement), pages 14-23, Berlin-Gtittingen-Heidelberg, 1950). They may also be obtained by reduction or catalytic hydrogenation of the appropriate 2-nitrophenylureas.

The isothiocyanates used as starting materials are defined by the Formula III, in which, as in Formula I, R stands preferably for methyl, ethyl or propyl. Some of the isothiocyanates are known [see J. Chem. Soc. 93, 696 (1908)]; they can also be obtained from the reaction between alkali metal isothiocyanates and haloformic acid esters. Suitable isothiocyanates include methoxycarbonylisothiocyanate, ethoxycarbonylisothiocyanate and propoxycarbonylisothiocyanate.

As diluents, when carrying out the process according to the invention all inert organic solvents are suitable. These include for example hydrocarbons, such as benzine', ligrion, hexane, benzene and toluene; chlorinated hydrocarbons, such as methylene chloride, chloroform, carbon tetrachloride and chlorobenzene; others, such as diethyl ether, dibutyl ether, tetrahydrofuran and dioxane; ketones, such as acetone, methylisopropyl ketone, acetophenone and cyclohexanone; and any desired mixtures of the said solvents.

The reaction temperature can be varied within a fairly wide range. In general, the work is carried out at from substantially between about 10 to 60 C., preferably from between about 0 to 40 C.

When carrying out the process according to the invention, 1 mole of isothiocyanate is preferably used per mole of the 2-ureidoaniline derivative. Amounts greater or lesser by up to 20% are possible without substantial diminution of the yield. When the reaction mixture is cooled, the end products are obtained in crystalline form and can be separated by suction filtration and, optionally, purified by redissolving or recrystallization. A preferred embodiment of the process comprises preparing the isothiocyanate in an inert solvent and reacting it directly, without further isolation, with the o-phenylenediamine derivative.

The active compounds according to invention exhibit a strong fuugitoxic activity. In the concentrations necessary for the control of fungi, they do not damage cultivated plants, and have a low toxiciy to warm-blooded animals. For these reasons, they are suitable as crop protection agents for the control of fungi. Fungitoxic agents in crop protection are used for the control of Archimycetes, Phycomycetes, Ascomycetes, Bmidiomycetes and Fungi imperfecti.

The active compounds according to the invention have a very broad activity spectrum and can be applied against parasitic fungi which infect above-the-soil parts of plants or attack the plants from the soil, as well as against seedbome pathogenic agents.

They are particularly effective against fungi which cause powdery mildew diseases. To this group of fungi there belong predominantly representatives from the Eryts'iphaceae family with the most important genera being Erysiphe, Unc inula (Oidium), Sphaerotheca and Podosphaera. Important fungi include Erysiphe cichoracearum, Podosphaera leucotricha and Uncinula necator.

The active compounds according to the invention also give good results in the control of rice diseases. Thus, they show an excellent activity against the fungi Piricularia oryzae and Pellicularia sasakii, by reason of which they can be used for the joint control of these two diseases. This means a substantial advance, since, up to now, agents of different chemical constitution were required against these two fungi. Surprisingly, the active compounds show not only a protective activity, but also a curative and systemic effect.

The compounds according to the invention, however, also act against other fungi which infect rice or other cultivated plants, such as Cochliobolus myiabeanus, Mycosphaerella musicola, Cerocospora personata, Botrytis cinerea, Alternaria species, Verticillium alboatrum, Phiwlophora cinerescens and Fusarium species, as well as against bacterium Xanthomonas oryzae.

The active compounds according to the instant invention cna be utilized, if desired, in the form of the usual formulations or compositions with conventional inert (i.e.

plant compatible or herbicidally inert) pesticide diluents or extenders, i.e. diluents or extenders of the type usable in conventional pesticide formulations or compositions, e.g. conventional pesticide dispersible carrier vehicles, such as solutions, emulsions, suspensions, emulsifiable concentrates, spray powders, pastes, soluble powders, dusting agents, granules, etc. There are prepared in known manner, for instance by extending the active compounds with conventional pesticide dispersible liquid diluent carriers and/or dispersible solid carriers optionally with the use of carrier vehicle assistants, e.g. conventional pesticide surface-active agents, including emulsifying agents and/or dispersing agents, whereby for example, in the case where water is used as diluent, organic solvents may be added as auxiliary solvents. The following may be chiefly considered for use as conventional carrier vehicles for this purpose: inert dispersible liquid diluent carriers including inert organic solvents, such as aromatic hydrocarbons (e.g. benzene, toluene, xylene, etc.), halogenated, especially chlorinated, aromatic hydrocarbons (e.g. chlorobenzenes, etc.), parafiins (e.g. petroleum fractions), chlorinated aliphatic hydrocarbons (e.g. methylene chloride, etc.), alcohols (e.g. methanol, ethanol, propanol, butanol, etc.), amines (e.g. ethanolamine, etc.), ethers, ether-alcohols (e.g. glycol monomethyl ether, etc.), amides (e.g. dimethyl formamide, etc.), sulfoxides (e.g. dimethyl sulfoxide, etc.), ketones (e.g. acetone, etc.), and/or water; as well as inert dispersible finely divided solid carriers, such as ground natural minerals (e.g. kaolins, alumina, silica, chalk, i.e. calcium carbonate, talc, kieselguhr, etc.) and ground synthetic minerals (e.g. highly dispersed silicic acid, silicates, e.g. alkali silicates, etc.); whereas the following may be chiefly considered for use as convention-a1 carrier vehicle assistants, e.g. surface-active agents, for this purpose: emulsifying agents, such as nonionic and/or anionc emulsifying agents (e.g. polyethylene oxide esters of fatty acids, polyethylene oxide ethers of fatty alcohols, alkyl sulfonates, aryl sulfonates, etc., and especially alkyl aryl-polyglycol ethers, magnesium stearate, sodium oleate, etc.); and/or dispersing agents, such as ligm'n, sulfite waste liquors, methyl cellulose, etc.

Such active compounds may be employed alone or in the form of mixtures with one another and/or with such solid and/or liquid dispersible carrier vehicles and/or with other known compatible active agents, especially plant protection agents, such as other fungicides, or herbicides, insecticides, bactericides, etc., if desired, or in the form of particular dosage preparations for specific application made therefrom, such as solutions, emulsions, suspensions, powders, pastes, and granules which are thus ready for use.

As concerns commercially marketed preparations, these generally contemplate carrier composition mixtures in which the active compound is present in an amount substantially between about 01-95%, and preferably 2-90% by weight of the mixture, whereas carrier composition mixtures suitable for direct application or field application generally contemplate those in which the active compound is present in an amount substantially between about 0.0001-%, preferably 0.01-1%, by weight of the mixture. Thus, the present invention contemplates over-all compositions which comprise mixtures of a conventional dispersible carrier vehicle such as (1) a dispersible carrier solid, and/or (2) a dispersible carrier liquid such as an inert organic solvent and/or water preferably including a surface-active effective amount of a carrier vehicle as sistant, e.g. a surface-active agent, such as an emulsifying agent and/or a dispersing agent, and an amount of the active compound which is effective for the purpose in question and which is generally about 0.0001-95%, and preferably 0.01-95 by weight of the mixture.

In the case of use as seed dressings, applied amounts of 0.1 to 10 g., preferably 0.2 to 2- g., of active compound per kg. of seed are suitable.

In the case of use as soil-treatment agents, applied amounts of 1 to 500 g., preferably 10 to 200 g. per cubic meter of soil are usually necessary.

The active compounds according to the invention also show an insecticidal and acaricidal activity as well as an activity against some mold fungi and yeasts. In concentration higher than those necessary for fungicidal activity, the substances inhibit plant growth.

The active compound can also be used in accordance with the well-known ultra-low-volume process with good success, i.e. by applying such compound if normally a liquid, or by applying a liquid composition containing the same, via very effective atomizing equipment, in finely divided form, e.g. average particle diameter of from 50- 100 microns, or even less, i.e. mist form, for example by airplane crop spraying techniques. Only up to at most about a few liters/hectare are needed, and often amounts only up to about 1 quart/acre, preferably 2-16 fiuid ounces/acre, are suflicient. In this process it is possible to use highly concentrated liquid compositions with said liquid carrier vehicles containing from about 20 to about 80 or by weight of the active compound, or even the active substance alone, e.g. about 20-100% by weight of the active compound.

In particular, the present invention contemplates methods of selectively killing, combating or controlling fungi, which comprises applying to at least one of (a) such fungi and (b) their habitat, i.e. the locus to be protected, a fungicidally effective or toxic amount of the particular active compound of the invention alone or together with a carrier vehicle as noted above. The instant formulations or compositions are applied in the usual manner, for instance by squirting, spraying, atomizing, vaporizing, scattering, dusting, fumigation, watering, sprinkling, pouring, dressing, incrustations, and the like.

It will be realized, of course, that the concentration of the particular active compound utilized in admixture with the carrier vehicle will depend upon the intended application. Therefore, in special cases, it is possible to go above or below the aforementioned concentration ranges.

The fungicidal effectiveness of the new compounds of the present invention is illustrated, without limitation, by the following examples.

EXAMPLE 1 Erysiphe test Solvent: 4.7 parts by weight acetone Emulsifier: 0.3 part by weight alkylaryl polyglycol ether Water: 95.0 parts by weight The amount of the active compound required for the desired concentration of active compound in the spray liquid is mixed with the stated amount of the solvent, and the concentrate is diluted with the stated amount of water containing the stated additions.

Young cucumber plants with about three foilage leaves are sprayed with the spray liquid until dripping wet. The cucumber plants remain in a greenhouse for 24 hours to dry. They are then, for the purpose of inoculation, dusted with conidia of the fungus Erysiphe cichoracearwm. The plants are subsequently placed in a greenhouse at 2324 C. and at a relative atmospheric humidity of about 75%.

After 12 days, the infection of the cucumber plants is determined as a percentage of the untreated but also inoculated control plants. 0% means no infection; 100% that the infection is exactly as great as in the case of the control plants.

The active compounds, the concentrations of the active compounds and the results obtained can be seen from the following Table 1.

TABLE 1 Erysiphe test Infection as a percentage of the infection of the un treated control with a concentration of active compound 01-] Active compound 0.025% 0. 0062% G Hr-NH-C S Z n C Hr-NH-CS (known) NHC-NH--C 0 0 CaHa NH-O-NH-CE NH--NH-C O 0 GaHl N H-CNHN NH-O-NH-G O 0 Calls N H-C-N H(CHz)|CN NH-C-NH-C 0 0 02H; NHCNHC III-Q NH-C-NH-C O O 02H;

(6).; H :ztr-zzz:

NHCNHC O 0 02H:

NH-fiJ-NHP-CHz-C Hr-OC H;

EXAMPLE 2 Piricularia and Pellicularia test Solvent: 4 parts by weight acetone Dispersing agent: 0.05 parts by weight sodium oleate Water: 95.75 parts by weight Other additives: 0.2 parts by weight gelatin about 70% until they are dry. One batch of the plants is then inoculated with an aqueous suspension of 100,000 to 200,000 spores/ml. of Piricularia oryzae and placed in a chamber at 24-26 C. and relative atmospheric humidity. The other batch of the plants is infected with a culture of Pellicularia sasakii grown on malt agar and placed at 28-30 C. and 100% relative atmospheric humidity.

5 to 8 days after inoculation, the infection of all the leaves present at the time of inoculation with Piricularia oryzae is determined as a percentage of the untreated but also inoculated control plants. In the case of the plants infected with Pellicularia sasakii, the infection on the leaf sheaths after the same time is also determined in proportion to the untreated but infected control. 0% means no infection; 100% means that the infection is exactly as great in the case of the control plants.

The active compoundsfthe concentrations of the active compounds and the results obtained can be seen'from the following Table 2.

dressing, the seed is shaken with the dressing in a closed glass flask. The seed, on moist loamunder-a cover of a layer of muslin and 2 cm. of moderately moist com- TABLE 2 Piricularla (a) and Pellicularia (b) test [Pr. =protective; Cur.=curative] Infection as a percentage of the infection of the untreated control with a concentration of active compound (in percent) EXAMPLE 3 Seed dressing test/bunt of wheat (seed-borne mycosis) To produce a suitable dry dressing, the active compound is extended with a mixture of equal parts by 70 weight of talc and kieselguhr to give a finely powdered mixture with the desired concentration of the active compound.

Wheat seed is contaminated with 5 g. of the chlamydospores of T illetia caries per kg. of seed. To apply the 75 TABLE 3 7 Seed dressing test/bunt of wheat Cone. of

active Amount Spore compound of dressgermiln dressing ing apnation in percent plied in in by weight g.[kg. seed percent Non-dressed- 10 Active compound (A).-- CHi-NH-O 8-8 10 1 5 /Zn CHz-NH-C S S (known) (4);: 3 30 1 0. 5

NH-C NHC O Calls NH-G-NH-Gm-Q .1: 1 0. 05 4]: 30 1 0. 005 NH- NHC O 0 01H:

(6);: 10 1 0. 05 a 30 1 0. 000 NH- -NHC 0 0 Cam NHCNHCH:CHaO-CH3 NH-PJ-NH-C 0 0 0211s NH-C-NHC H:

NH-iJ-NH-C 0 O 01H:

NH--CNHN CH: CH;

EXAMPLE 4 Mycellium growth test Nutrient substrate used:

parts by weight agar-agar (powdered) parts by weight malt extract 950 parts by weight distilled water Proportion of solvent to nutrient substrate:

2 parts by weight acetone 100 parts by weight agar nutrient substrate The amount of active compound required for the desired concentration of active compound in the nutrient substrate is mixed with the stated amount of solvent. The concentrate is thoroughly mixed in the stated proportion with the liquid nutrient substrate (which has been cooled to 42 C.) and poured into Petri dishes with a diameter 0 No growth of fungus.

1 Very strong inhibition of growth. 2 Moderate inhibition of growth.

3 Slight inhibition of growth.

4 Growth equal to untreated control.

sterilized and then inoculated with pure cultures of the The active compounds, concentrations of active, comtest fungi. p pounds and the results obtained can be seen from the The soil is filled into 5 pots, each of which is sown with following Table 4: 10 seeds of the host plants. The pots are placed in a green- TABLE 4 Mycelium growth test Concentra- Fungi tion of active Pellicu- Verticil- Phialo- Cerco- Piricu compound Zaria salium albophora cinspora laria Active compound in p.p.m. sakii atrum erescens musae oryzae (A)--- cH,-NH-c 8-5 10 4 3 4 3 4 Zn OHr-NH-C s -s (known) NHCNHC O O C2H5 1 s 10 o o o o Nn-t i-Nn-o o 0 02115 NHC-NH--CH:

mr-t L-Nn-coooem CH3 @NHCNHN/ g CHs @NH-ii-NH-o o 0 02H! NHCNH(CHz)5-CN 5 s o o o o EXAMPLE 5 house at the stated temperatures and kept normally moist. S treating agent test/soil-borne mywses 3 weeks after sowing, the number of healthy plants is determined as a percentage of the number of seeds sown. To Produce Sultable prepfiratlon of eefl 0% means that no healthy plants have grown; 100% Pound, the actlve compound 15 extended Wlth talc to a means that healthy plants have resulted from all the seeds.

content of 5% and subsequ n y With quartz Sand a The active compounds, the concentrations of the active content of 0.5% of actlve compound. I compounds in the soil, the test fungi, host plants, green- The preparation of the active compound is uniformly house temperatures and the results obtained can be seen mixed with Fruhstorfer standard soil, which has first been from the following Table 5:

TABLE Soil treating agent test/soil-borne myeoses [Test fungi=Fusarium culmarum-Host plant=pea-temperature range=2225] Concentration of acti compound,

mgJliter soil Results Fruhstorfer standard soil, sterilized untr Fruhstorfer standard soil, sterilized and inoculated untreated Active compound CHa-NH-C S -S (2).:m3zzzzz: 8 ll s II II c EXAMPLE 6 Erysiphe test/systemic Solvent: 4.7 parts by weight acetone Emulsifier: 0.3 part by weight alkylaryl polyglycol ether Water: 95 parts by weight The amount of the active compound required for the desired concentration in the liquid to be used for watering is mixed with the stated amount of the solvent, and the concentrate is diluted with the stated amount of water containing the stated additions.

Cucumber plants grown in standard soil are, in the oneto two-leaf stage, waterd three times in one week with cc. of the liquid to be used for watering, in the stated concentration of active compound with reference to 100 cc. of soil.

The plants so treated are, after the treatment, inoculated with conidia of the fungus Erysiphe cichoracearum. The plants are subsequently placed in a greenhouse at 23-24 C. and at a relative atmospheric humidity of 70%.

After 12 days, the infection of the cucumber plants is determined as a percentage of the untreated but also inoculated control plants. 0% means no infection; 100% means that the infection is exactly as great as in the case of the control plants.

The active compounds, the concentrations of the active compounds and the results obtained can be seen from the following Table 6:

TABLE 6 Active compound II CHr-NH-C-S nown) II NH-C-NH-C O 0 C211;

Infection as a percentage of the infection of the untreated control with a concentration of active compound of 120 p.p.m.

17 EXAMPLE 7 Podosphaera test (powdery mildew of apples) [protective] Solvent: 4.7 parts by weight acetone Emulsifier: 0.3 part by weight alkylaryl polyglycol ether Water: 95 parts by weight main in a greenhouse for 24 hours at 20 C. and at a relative atmospheric humidity of They are then inoculated by dusting with conidia of the apple powdery mildew causative organism (Podosphaera leucolricha Salm.) and placed in a greenhouse at a temperature of 21-23 C. and at a relative atmospheric humidity of about 70%.

Ten days after the inoculation, the infestation o the seedlings is determined as a percentage of the untreated but also inoculated control plants.

0% means no infestation; means that the infestation is exactly as great as in the case of the control plants.

The active compounds, the concentrations of the active compounds and the results obtained can be seen from the following Table 7:

TABLE 7 Podosphaera test/protective Infection as a percentage of the infection of the untreated control with a concentration of actlve compound of- Aetive compound 0. 0062% 0. 00156% CHPNH(%-S CHr-NHCS (known) NH C NH-C O O CzHr NH-C-NH-CHz-Q NH( J-NHC O O CaHl N H-C-NH- NH--NHF-C O O C211 N H-C-NH-CHr-CHr-O-CH:

@NH-(i-NH-o o 0 mn- NHC--NHC H:

NH-( NH-C O O CzHl CH3 N HCNHN y) C H:

3,780,089 19 20 EXAMPLE 8 EXAMPLE 9 Podosphaera test (systemic) Solvent: 4.7 parts by weight acetone Dispersing agent: 0.3 part by weight alkylaryl polyglycol Solvent: Parts y Welght acetone Fusicladium test (apple scab) [curative] ether Emulsifier: 0.3 part by weight alkylaryl polyglycol ether Water: 95 parts by weight Water: 95 parts by weight The amount 9 active 9 required the The amount of active compound required for the deslred concentration of the aetwe compound In the sired concentration of the active compound in the spray to be used for watering is mixed i i stated 10 liquid is mixed with the stated amount of solvent, and the amount of solvent, and the concentrate is diluted with concentrate is diluted with the stated amount of water the stated amount of water which contains the stated adwhich contains the stated additions ditions' Young apple seedlings in the 4-6 leaf stage are Apple Seedhngs Standard 501,1 m the 3-4 inoculated with an aqueous conidium suspension of the leaf Stage watered once one week with 20 of the apple scab causative organism Fusicladium dendriticum liquid to used for wateriPg in the stated eeneenn'a' el and incubated for 18 hours in a humidity chamber acme P wlth reference 9- at '18-20 c. and at an atmospheric humidity of 100%. $011. The plants so treated are, after the treatment, moc- The plants are then placed in a greenhouse where they ulated with conidia of Podosphaera leucotricha Salm and placed in a a temPefamre of 2143, 20 After standing for a suitable period of time, the plants and at a relative atmospheric humidity of about 70% 10 are Sprayed dripping wet with the spray liquid prepared gays aftel: the Inoculation the m'feetlon of the seedlmgs in the manner described above. The plants are subsequent- 13 determined as a percentage of the untreated but also 1y placed in a greenhouse.

Inoculated control. i fl h inf 15 days after inoculation, the infestation of the apple means no mfectlo? 100% means that t e seedlings is determined as a percentage of the untreated tion s exactly as great as in the case of the control plants. but also inoculated control plants.

The acme g a zg g i g ofbthe 0% means no infestation; 100% means that the infestai i ge ts o tame can e Seen tion is exactly as great as in the case of the control plants. om t e o owmg a e The active compounds, the concentrations of the active TABLE 3 compounds, the period of time between inoculation and Podosphaera test/systemic spraying and the results obtained can be seen from the fol- Imecmm as a lowing Table 9: percentage 01 the infection 0! the untreated control with :1! TABLE 9 aiiiv e fififigfi ufld Fusieladium test/curative Active compound of 120 p.p.m. [Residence D8 110 d of 42 hours] f: 100 40 Infectiotn as at ercen B B0 CHa-NH S tl ie infectiem of Zn the untreated control with a HrNH-CS concentration H of active compound of Active compound 0.1% (A)--. s 75 fi om-NH-o-s nn-o-mn-oooclm (L Zn HaNH-C-S nn-c-nn-om-Q g (L (known) 1a 5 NH .Q. NH C 0 o CIH -NH--NH-C O 0 CzHi NH-ENHOHr-CH:OCHI "E- (I)... S 12 e S 6 (2)... s a (6).... s o

TABLE 9-'Continued Infection as a percentage of the infection of the untreated control with a concentration of active compound Active compound of 120 p.p.m.

EXAMPLE 10 Fusicladium test (systemic) The amount of active compound required for the desired concentration of the active compound in the liquid to be used for watering is mixed with the stated amount of solvent, and the concentrate is diluted with the stated amount of Water which contains the stated additions.

Apple seedlings grown in standard soil are, in the 3-4 leaf stage, watered once in one week with cc. of the liquid to be used for watering, in the stated concentration of active compound, with reference to 100 cc. of soil. The plants so treated are, after the treatment, inoculated with an aqueous conidium suspension of Fusicladiwm. dendriticum el and incubated for 18 hours in a humidity chamber at 18-20 C. and at a relative atmospheric humidity of 100%. The plants are subsequently placed in a greenhouse for 14 days.

15 days after inoculation, the infection of the seedlings is determined as a percentage of the untreated but also inoculated control plants. 0% means no infection; 100% means that the infection is exactly as great as in the case of the control plants.

The active compounds, the concentrations of the active compounds and the results obtained can be seen from the following Table 10:

TABLE 10 Fusicladium test/systemic Infection as a percentage of the infection of the untreated control with a concentration of active compound Active compound of 120 p.p.m.

CHa-NH-O-S Zn Hz-NH(||3-S (known) I NHNH-C 0 0 C2Hs -NH- NH-om- TABLE 10Continued Active compound of ppm.

NH-C-NH-C O 0 02115 NH-fl-NH-CH:

The following examples are set forth to illustrate, without limitation, the process for producing the compounds of the present invention.

EXAMPLE 11 45.4 (0.2 mole) N-2 aminophenyl-N'-phenylurea in 200 cc. dry chloroform are provided. 26.2 g. (0.2 mole) ethoxycanbonyl isothiocyanate are added dropwise, the temperature being kept at 30 C. by cooling with ice. After further stirring for one hour, suction filtration is eifected. Yield: 68 g. (96% of theory) N-[2-(phenyluredio)- phenyl]-N'-ethoxycarbonylthiourea which can be purified by recrystallization from acetonitrile/dimethylformamide; the melting point of the pure compound is 172- 175 C. (with decomposition). In analogous manner, the following compounds were obtained:

Melt i Formula C.) p0 nt (4)"... 176-9 (decomp.)

It will be realized by the artisan that all of the foregoing oompounds contemplated by the present invention possess the desired strong fungicidal properties, with regard to a broad spectrum of activity, as well as a comparatively low toxicity toward warm-blooded creatures and a concomitantly low phytotoxicity, enabling such compounds to be used with correspondingly favorable compatibility with respect to warm-blooded creatures and plants for more effective control and/or elimination of fungi by application of such compounds to such fungi and/ or their habitat.

It will be appreciated that the instant specification and examples are set forth by way of illustration and not limitation, and that various modifications and changes may be made without departing from the spirit and scope of the present invention.

24 What is claimed is: 1. A ureidophenyl thiourea of the formula It 3 R" in which R stands for alkyl with 1-12 carbon atoms, R and R" each stands independently for a hydrogen atom or alkyl with 1-4 carbon atoms, and R' stands for alkyl with up to 18 carbon atoms substituted with alkoxy with up to 4 carbon atoms.

2. A urea according to claim 1, in which R stands for methyl, ethyl or propyl; R and R" each stands independently for hydrogen, methyl or ethyl; and R' stands for methoxyethyl or ethoxypropyl.

3. A urea according to claim 1, in which R stands for ethyl; R and R" each stands independently for hydrogen or methyl; and R'" stands for lower alkyl substituted by lower alkoxy.

4. A compound according to claim 1, wherein such compound is N-[2 (methoxyethylureido)-phenyl]-N'- ethoxycarbonylthiourea of the formula References Cited FOREIGN PATENTS 4,519,078 3/1970 Japan 268470 1,054,777 4/1959 Germany 260470 1,191,406 5/ 1970 Great Britain 260-470 694,362 1/1970 Republic of South Africa LORRAINE A. WEINBERGER, Primary Examiner I. F. TERAPANE, Assist-ant Examiner US. Cl. X.R. 

